Diagnosis of osteoporosis in statin-treated patients is dose-dependent

被引:60
|
作者
Leutner, Michael [1 ]
Matzhold, Caspar [2 ,3 ]
Bellach, Luise [1 ]
Deischinger, Carola [1 ]
Harreiter, Juergen [1 ]
Thurner, Stefan [2 ,3 ,4 ,5 ]
Klimek, Peter [2 ,3 ]
Kautzky-Willer, Alexandra [1 ]
机构
[1] Med Univ Vienna, Unit Gender Med, Clin Div Endocrinol & Metab, Dept Internal Med 3, Vienna, Austria
[2] Med Univ Vienna, CeMSIIS, Sect Sci Complex Syst, Vienna, Austria
[3] Complex Sci Hub Vienna, Vienna, Austria
[4] Santa Fe Inst, Santa Fe, NM 87501 USA
[5] IIASA, Laxenburg, Austria
关键词
HORMONE-BINDING GLOBULIN; TESTOSTERONE LEVELS; BONE-DENSITY; RISK; SIMVASTATIN; FRACTURES; ASSOCIATION; INHIBITORS; REDUCTASE; DECREASE;
D O I
10.1136/annrheumdis-2019-215714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Whether HMG-CoA-reductase inhibition, the main mechanism of statins, plays a role in the pathogenesis of osteoporosis, is not entirely known so far. Consequently, this study was set out to investigate the relationship of different kinds and dosages of statins with osteoporosis, hypothesising that the inhibition of the synthesis of cholesterol could influence sex-hormones and therefore the diagnosis of osteoporosis. Methods Medical claims data of all Austrians from 2006 to 2007 was used to identify all patients treated with statins to compute their daily defined dose averages of six different types of statins. We applied multiple logistic regression to analyse the dose-dependent risks of being diagnosed with osteoporosis for each statin individually. Results In the general study population, statin treatment was associated with an overrepresentation of diagnosed osteoporosis compared with controls (OR: 3.62, 95% CI 3.55 to 3.69, p<0.01). There was a highly non-trivial dependence of statin dosage with the ORs of osteoporosis. Osteoporosis was underrepresented in low-dose statin treatment (0-10 mg per day), including lovastatin (OR: 0.39, CI 0.18 to 0.84, p<0.05), pravastatin (OR: 0.68, 95% CI 0.52 to 0.89, p<0.01), simvastatin (OR: 0.70, 95% CI 0.56 to 0.86, p<0.01) and rosuvastatin (OR: 0.69, 95% CI 0.55 to 0.87, p<0.01). However, the exceeding of the 40 mg threshold for simvastatin (OR: 1.64, 95% CI 1.31 to 2.07, p<0.01), and the exceeding of a 20 mg threshold for atorvastatin (OR: 1.78, 95% CI 1.41 to 2.23, p<0.01) and for rosuvastatin (OR: 2.04, 95% CI 1.31 to 3.18, p<0.01) was related to an overrepresentation of osteoporosis. Conclusion Our results show that the diagnosis of osteoporosis in statin-treated patients is dose-dependent. Thus, osteoporosis is underrepresented in low-dose and overrepresented in high-dose statin treatment, demonstrating the importance of future studies' taking dose-dependency into account when investigating the relationship between statins and osteoporosis.
引用
收藏
页码:1706 / 1711
页数:6
相关论文
共 50 条
  • [31] CLINICAL DETERMINANTS OF INCIDENT AORTIC STENOSIS IN STATIN-TREATED STABLE CORONARY PATIENTS
    Arsenault, Benoit
    Boekholdt, Matthijs
    Mora, Samia
    DeMicco, David
    Bao, Warren
    Deedwania, Prakash
    Tardif, Jean Claude
    LaRosa, John C.
    Barter, Philip
    Waters, David
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 61 (10) : E1950 - E1950
  • [32] Safety and tolerability of prolonged-release nicotinic acid in statin-treated patients
    Birjmohun, R. S.
    Kastelein, J. J. P.
    Poldermans, D.
    Stroes, E. S. G.
    Hostalek, U.
    Assmann, G.
    CURRENT MEDICAL RESEARCH AND OPINION, 2007, 23 (07) : 1707 - 1713
  • [33] Lipid risk factors for vascular events in statin-treated diabetic coronary patients
    Drexel, Heinz
    Aczel, Stefan
    Marte, Thomas
    Schmid, Fabian
    Koch, Lorena
    Langer, Peter
    Rein, Philipp
    Hoefle, Guenter
    Saely, Christoph H.
    DIABETES, 2007, 56 : A180 - A180
  • [34] Targeting High-Density Lipoprotein and Triglycerides in Statin-Treated Patients with Diabetes
    Bonds D.E.
    Current Cardiovascular Risk Reports, 2012, 6 (1) : 102 - 107
  • [35] Dyslipidemia among statin-treated patients experiencing cardiovascular and cerebrovascular events in the UK
    Phatak, H.
    Wentworth, C.
    Beetsch, J.
    Sazonov-Kocevar, V.
    ATHEROSCLEROSIS SUPPLEMENTS, 2007, 8 (01) : 125 - 125
  • [36] PROTEOMICS DISCOVERY OF BIOMARKERS IN STATIN-TREATED PATIENTS WITH ADVANCED CORONARY ARTERY DISEASE
    Tzani, Aspasia
    Doulamis, Ilias
    Konstantopoulos, Panagiotis
    Antoranz, Asier
    Pliaka, Vaia
    Minia, Aggeliki
    Gkogkos, Anastasios
    Samanidis, George
    Sakellaropoulos, Theodore
    Alexopoulos, Leonidas
    Perrea, Despina
    Perreas, Konstantinos
    ATHEROSCLEROSIS, 2017, 263 : E241 - E241
  • [37] Myopathy in Statin-Treated Children and Adolescents: A Practical Approach
    Kavey, Rae-Ellen W.
    CURRENT ATHEROSCLEROSIS REPORTS, 2024, 26 (12) : 683 - 692
  • [38] DOSE-DEPENDENT AND TIME-DEPENDENT HYDROCEPHALUS IN RATS TREATED WITH IDPN
    FIORI, MG
    SHARER, LR
    LOWNDES, HE
    NEUROTOXICOLOGY, 1984, 5 (02) : 305 - 305
  • [39] Persistent dyslipidemia in statin-treated patients: The focus on comprehensive lipid management survey in Swiss patients
    Sudano, Isabella
    Hess, Lorenzo
    Noll, Georg
    Arnet, Diana
    SWISS MEDICAL WEEKLY, 2011, 141
  • [40] Immortal Time Bias Can Occur in the Analysis of Dose-Dependent Effect of Statin
    Lin, Chun-Yu
    CHEST, 2018, 153 (06) : 1508 - 1509